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familial apolipoprotein C-II deficiency

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


Uniprot Description Autosomal recessive trait characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis and early atherosclerosis.
Mondo Term and Equivalent IDs
MONDO:0008810:  familial apolipoprotein C-II deficiency
DOID:0111418: 
Orphanet:309020: 
SCTID:33513003: 
UMLS:C0268199: 
UMLS:C1720779: